Denys-Drash Syndrome
Disease ID: disease_node_11040
Connections displayed (default: 10).
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| Dbxref | GARD:5576, MESH:D030321, MIM:194080, NCI:C84668, SNOMEDCT_US_2023_03_01:236385009, UMLS_CUI:C0950121 |
|---|---|
| Subclassof | DOID_0050736, DOID_225 |
| Data Source | DOID, MESH |
| Mesh Id | D030321 |
| Mesh Label | Denys-Drash Syndrome |
| Mesh Subclassof | D058490, D009396 |
| Doid Label | Denys-Drash syndrome |
| Doid Description | A syndrome that is characterized by the association of diffuse mesangial sclerosis (DMS), male pseudohermaphroditism with a 46,XY karyotype, and nephroblastoma that derives_from an abnormality in the WT1 gene (Wilms' tumor suppressor gene). OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_11040 |
| Doid Id | DOID_3764 |
| Label | Denys-Drash Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)